Pure Global

Rotavirus Antigen Rapid Test - India CDSCO Medical Device Registration

Rotavirus Antigen Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_4a2ed071ae55ce8d826640b1f1670921_679e7da5b45adf5256931c92c9731a14. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Rotavirus Antigen Rapid Test
UID: MFG/IVD/2022/000056_4a2ed071ae55ce8d826640b1f1670921_679e7da5b45adf5256931c92c9731a14

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Rotavirus Ag Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of rotavirus antigen in fecal specimens

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from Biotrol Laboratories Pvt. Ltd.
Products from the same license holder (10 products)

H. Pylori Ag Rapid Test

Class C

Procalcitonin Ag Rapid Test

Class C

HBsAg Rapid Test

Class D

Vibrio Cholera Ag Rapid Test

Class C

Malaria PF/PAN Ag Rapid Test

Class C

Troponin I Rapid Test

Class C

Dengue NS1 Antigen Rapid Test

Class C

Rota and Adenovirus Antigen Rapid Test Kit

Class C

HIV 1/2 Rapid Test Device

Class D

HCV Rapid Test

Class D